CN101370469A - Hair treatment compositions - Google Patents
Hair treatment compositions Download PDFInfo
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- CN101370469A CN101370469A CNA2006800527032A CN200680052703A CN101370469A CN 101370469 A CN101370469 A CN 101370469A CN A2006800527032 A CNA2006800527032 A CN A2006800527032A CN 200680052703 A CN200680052703 A CN 200680052703A CN 101370469 A CN101370469 A CN 101370469A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
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Abstract
The invention provides a hair treatment composition comprising a combination of a sugar, an amine oxide and an amino acid. The composition is particularly suitable for the treatment of hair which is dry, damaged and/or prone to manageability problems.
Description
Invention field
The present invention relates to a kind of hair-treatment composition, it comprises sugar, amine oxide and amino acid whose combination.Described compositions is specially adapted to drying, impaired and/or be prone to the processing of the hair of the problem of arranging.
Background and prior art
Hair can be impaired because of multiple factor.For example, the environmental factors that hair is impaired comprises contact UV and chlorine.The impaired chemical factor of hair for example comprise bleach, the processing of permanent hair styling and straightening, and use coarse surfactants based cleaning shampoo compositions to have one's hair wash too continually.The impaired mechanical factor of hair comprises and too stroking and combing hair, and crosses long-time heating apparatus drying and the shaping hair of using.
Hair damage is usually expressed as hair fiber loss of epidermis layer and albumen, hair fiber drying, hair fiber is fragile and rupture and send out wearing and tearing or bifurcated slightly.Dry damaged hair is easy to generate the problem of arranging especially, produces for example situation of " frivolous (flyaway) " hair, and this hair is difficult to molding maybe can not keep moulding, particularly under environment such as high humidity.
Multiple organic molecule and combination thereof have been proposed to be used in handles dry, the impaired and/or difficult hair of arranging.
For example, WO 2004054526 has described hair-treatment composition, is used for nursing and repairs damaged hair, and improve the easily property arranged of hair, and it comprises disaccharide (particularly trehalose) and diacid (particularly adipic acid).
WO 2004054525 has described hair-treatment composition, is used for nursing and repairs damaged hair, and improve the easily property arranged of hair, and it comprises disaccharide (particularly trehalose) and glycol (particularly 3-methyl isophthalic acid, 3-butanediol).
WO 2004006874 has described hair-treatment composition, is used to repair and prevent the cardinal symptom of damaged hair, and it comprises the amine of specific side chain and/or hydroxy compounds (particularly 3,3-dimethyl-1,2-butanediol).
WO 2002015852 has described and has been used for repairing and atraumatic hair-treatment composition, and it comprises short chain oxidative amination compound, for example trimethyl amine oxide.
The present invention finds, the hair-treatment composition that comprises sugar, amine oxide and aminoacid combination can more effectively be handled drying, impaired and/or be prone to the hair of the problem of arranging.
Summary of the invention
The invention provides the hair-treatment composition that comprises sugar, amine oxide and aminoacid combination.
The present invention also provides above-mentioned composition to handle dry, the impaired and/or difficult purposes of arranging hair.
The present invention also provides above-mentioned composition has been applied to the method that hair comes treatment of hair.
Detailed Description Of The Invention and preferred implementation
Sugar
The present composition comprises at least a sugar.
" sugar " typically refers to monosaccharide, disaccharide and rudimentary oligosaccharide (comprising usually with banded 3 to 6 monosaccharide units of glycosidic bond).
The present invention preferably uses monosaccharide.Term " monosaccharide " (with respect to oligosaccharide or polysaccharide) is meant single unit, is not connected with other this unitary glucosides.
Monosaccharide has molecular formula (CH
2O)
n, wherein n can be arbitrary integer of 3 to 8.Monosaccharide comprises 2 to 7 hydroxyls (this depends on the number of carbon atom), and ketone group or aldehyde radical.
The monosaccharide that contains aldehyde radical is commonly referred to as " aldose ", and the monosaccharide that contains ketone group is commonly referred to as " ketose ".Preferred aldose.
Be used for preferred monosaccharide of the present invention and comprise 4,5,6 or 7 carbon atoms.Be respectively tetrose, pentose, hexose and heptose.
Because existence one triose (monosaccharide that contains three carbon atoms) of asymmetric carbon has an asymmetric carbon, other monosaccharide has several asymmetric carbon-every kind monosaccharide that several stereoisomer forms are all arranged, if triose, it can be an enantiomer; If other monosaccharide, it can be enantiomer and diastereomer.
Can be used for pentose of the present invention and hexose respectively cyclisation be furanose ring and pyranose ring.In aqueous medium, pentose and hexose mainly exist with annular form.
Can be used for preferred aldose of the present invention is: erythrose and threose (it is a tetrose), ribose, arabinose, xylose and lyxose (it is a pentose), and allose, altrose, glucose, mannose, gulose, idose, galactose and talose (it is a hexose).
Can be used for preferred ketose of the present invention is: Erythrulose (it is a tetrose), ribulose and xylulose (it is a pentose), psicose, fructose, sorbose and Tagatose (it is a hexose).
Ketose also can have annular form.For example, fructose can have the form of fructofuranose or fructopyranose.
Any mixture of above-mentioned substance also can be used in the present composition.
Preferably, the sugar that is used for the present composition is aldehyde sugar, most preferably galactose.
The total amount of sugar is generally 0.01 to 10% in the hair-treatment composition of the present invention, and is preferred 0.05 to 1%, more preferably from about 0.1% (based on the sugared gross weight of the total restatement of compositions).
Amine oxide
The present composition comprises at least a amine oxide.
The example of suitable oxidizing amine comprises:
(a) alkyl two-(low alkyl group) amine oxide, wherein alkyl has 6 to 24, and preferred 8 to 18, more preferably 8 to 12 carbon atoms can be straight or brancheds, and are saturated or undersaturated.Each low alkyl group comprises 1 to 7, preferred 1 to 3 carbon atom.More preferably, described low alkyl group all is a methyl.Embodiment comprises: octyldimethyl amine oxide, decyl dimethyl oxidation amine, dimethyl dodecyl amine oxide, CH3-(CH2)13N(CH3)2-O, and wherein alkyl is those materials of different amine oxide mixture, for example cacodyl oxide base coco amine, cacodyl oxide base (h-tallow) amine and myristyl/palmityl dimethyl amine oxide.
(b) alkyl two-[hydroxyl (low alkyl group)] amine oxide, wherein alkyl has 6 to 24, and preferred 8 to 18 carbon atoms can be straight or brancheds, and are saturated or undersaturated.Each hydroxyl (low alkyl group) group comprises 1 to 7, preferred 1 to 3 carbon atom.More preferably, described hydroxyl (low alkyl group) group all is an ethoxy.Embodiment comprises: oxidation two-(2-ethoxy) coco amine, oxidation two-(2-ethoxy) beef tallow amine and two-(2-ethoxy) octadecyl amine oxide.
(c) alkylamide propyl two-(low alkyl group) amine oxide, wherein alkyl has 10 to 20, and preferred 12 to 16 carbon atoms can be straight or brancheds, and are saturated or undersaturated.Each low-grade alkyl group comprises 1 to 7, preferred 1 to 3 carbon atom.More preferably, described low-grade alkyl group all is a methyl.Embodiment has: cocamidopropyl propyl amide dimethyl oxidation amine and Adeps Bovis seu Bubali amido propyl dimethyl oxidation amine.
(d) alkyl cyclammonium oxide, wherein alkyl has 10 to 20, and preferred 12 to 16 carbon atoms can be straight or brancheds, and are saturated or undersaturated, and cyclic group has 4 to 10 carbon atoms, can choose wantonly to comprise nitrogen or sulfur.Embodiment has: dialkyl group piperazine two-N-oxide and alkyl morpholine N-oxide, for example cetyl morpholine N-oxide and dodecyl morpholine N-oxide.
Any mixture of above-mentioned amine oxide also can be used in the present composition.
Being used for preferred amine oxide of the present invention is the alkyl two described in top (a)-(low alkyl group) amine oxide.Most preferred amine oxide is a decyl dimethyl oxidation amine.Such suitable material can be available from McIntyre Group, Ltd.'s
Series series, for example
065.
The total amount of amine oxide is generally 0.01 to 10% in the hair-treatment composition of the present invention, and is preferred 0.05 to 1%, more preferably from about 0.1% (based on the amine oxide gross weight of the total restatement of compositions).
Aminoacid
The present composition comprises at least a aminoacid.
Term " aminoacid " is meant and not only contains amino but also contain the molecule of carboxyl.Aminoacid can belong to L-or D-series or can be racemic.
The present invention preferably uses basic amino acid.Term " basic amino acid " is meant and contains the aminoacid of basic group (for example amino, amidino groups or guanidine radicals) more than carboxyl.The example of this basic amino acid has natural and non-natural diaminourea-monocarboxylic acid, α for example, β-diaminopropionic acid, alpha, gamma-DAB, lysine, arginine, histidine, ornithine and right-aminobenzene alanine.
Basic amino acid usually with the isolated in form of salt and hydrated salt (hydrosalts) from natural origin, it also is suitable for using in the present invention.This salt and hydrated salt (hydrosalts) by with mineral acid (for example hydrochloric acid, phosphoric acid, carbonic acid, sulphuric acid, nitric acid etc.), or organic acid (for example formic acid, acetic acid, dodecylic acid, monoxone etc.) reaction and forming.Suitable examples is an arginine hydrochloride.
Also can use other derivant, for example N-substitutive derivative and peptide derivant.These also can salt or the form of hydrated salt use.The example of N-substitutive derivative has N-alkyl acyl derivative and N-alkyl derivative.Usually, in the N-alkyl acyl derivative, alkanoyl has 3 to 20 carbon atoms, the alkyl chain length of preferred 4 to 10 carbon atoms, for example N-bytyry, N-caproyl and N-caprylyl.In the N-alkyl derivative, alkyl has 1 to 20 carbon atom, the alkyl chain length of preferred 1 to 4 carbon atom, for example methyl, ethyl and n-pro-pyl usually.The example of peptide derivant is that wherein the peptide residue comprises 2 to 8 amino acid residues or is substituted those materials of amino acid residue.
Any mixture of above-mentioned substance also can be used in the present composition.
Being used for preferred amino acid of the present invention is lysine, arginine, histidine, ornithine and composition thereof.Arginine most preferably.
Amino acid whose total amount is generally 0.01 to 10% in the hair-treatment composition of the present invention, and is preferred 0.05 to 1%, more preferably from about 0.1% (based on the aminoacid gross weight of the total restatement of compositions).
Product form
The appropriate format of hair-treatment composition of the present invention can be shampoo, regulator (conditioner), spraying, mousse, gel, wax or washing liquid.
Particularly preferred product form is shampoo, wash back regulator (conservative and wash type) and hair treatment product, for example hair oil and shampoo.
Shampoo compositions
Shampoo compositions of the present invention is generally aqueous, that is, they with water or aqueous solution or lysotropic liquid crystal as its key component.
Suitably, the water content of described shampoo compositions is 50 to 98%, and preferred 60 to 90% weight are based on total restatement of compositions.
The anion cleansing surfactants
Shampoo compositions of the present invention comprises one or more anion cleansing surfactants usually, and it is acceptable and be applicable to the hair topical application on the cosmetics.
Suitably the example of anion cleansing surfactants has: alkyl sulfate, alkyl ether sulfate, alkylaryl sulfonates, alkanoyl isethionate, alkyl succinate, alkyl sulfo succinate, alkyl ether sulfo succinate, N-alkyl sarcosine salt, alkylphosphonic, alkyl ether phosphate; with alkyl ether carboxylic acid and salt thereof, particularly its sodium salt, magnesium salt, ammonium salt and single-, two-and triethanolamine salt.Described alkyl and acyl group comprise 8 to 18 usually, preferred 10 to 16 carbon atoms, and can be undersaturated.Described alkyl ether sulfate, alkyl ether sulfo succinate, alkyl ether phosphate and alkyl ether carboxylic acid and salt thereof can comprise 1 to 20 oxirane or propylene oxide units in each molecule.
The typical anion cleansing surfactants that is used for shampoo compositions of the present invention comprises: the oleyl sodium succinate, dodecyl 2-Sulfosuccinic acid ammonium, sodium lauryl sulphate, sodium lauryl tri(oxyethyl) sulfate, the lauryl ether sodium sulfosuccinate, ammonium lauryl sulfate, ammonium dodecyl ether sulfate, dodecylbenzene sodium sulfonate, the DBSA triethanolamine, the cocoyl sodium isethionate, the dodecyl sodium isethionate, lauryl ether carboxylic acid and N-sarcosyl.
The preferred anionic surfactants cleansing surfactants is: sodium lauryl sulphate, sodium lauryl tri(oxyethyl) sulfate (n) EO (wherein n is 1 to 3), lauryl ether sodium sulfosuccinate (n) EO (wherein n is 1 to 3), ammonium lauryl sulfate, ammonium dodecyl ether sulfate (n) EO (wherein n is 1 to 3), cocoyl sodium isethionate and lauryl ether carboxylic acid (n) EO (wherein n is 10 to 20).
Any mixture of above-mentioned anion cleansing surfactants is also applicable.
The total amount of anion cleansing surfactants is generally 0.5 to 45% of compositions gross weight with the total restatement of anion cleansing surfactants in the shampoo compositions of the present invention, and is preferred 1.5 to 35%, and more preferably 5 to 20%.
Other composition
Randomly, shampoo compositions of the present invention can comprise following compositions, improves performance and/or consumer's acceptability.
Cosurfactant
Described compositions can comprise cosurfactant, obtains aesthetic, physics or sanitary characteristics to help compositions.
The example of cosurfactant is a non-ionic surface active agent, and its content can be 0.5 to 8%, and preferred 2 to 5% weight are with total restatement of compositions.
For example, the representative ionic surfactant pack that can be used for shampoo compositions of the present invention is drawn together: aliphatic (C
8-C
18) condensation product of the primary alconol of straight or branched or secondary alcohol or phenol and alkylene oxide (normally oxirane, and have 6 to 30 ethylene oxide groups usually).
That other representative ionic surfactant pack is drawn together is single-or two-alkyl chain triacontanol amide.Embodiment comprise cocoyl single-or two-glycollic amide and cocos nucifera oil list-isopropanol amide.
Other non-ionic surface active agent that can be used for shampoo compositions of the present invention is alkyl poly glucoside (APG).Usually, APG comprises with one or more glycosyl blocks (block) alkyl of link to each other (optional via bridging group).Preferred APG has following formula:
RO-(G)
n
Wherein R is a branched-chain or straight-chain alkyl, and it can be saturated or undersaturated, and G is a carbohydrate group.
R can represent about C
5To about C
20Mean alkyl chain long.Preferably, the about C of R representative
8To about C
12Mean alkyl chain long.Most preferably, the R value is about 9.5 to about 10.5.G can be selected from C
5Or C
6Monosaccharide residue, and be preferably glucoside.G can be selected from: glucose, xylose, lactose, fructose, mannose and derivant thereof.Preferred G is a glucose.
The degree of polymerization, the n value can be about 1 to about 10 or bigger.Preferably, the n value is about 1.1 to about 2.Most preferably, the n value is about 1.3 to about 1.5.
Being used for suitable alkyl poly glucoside of the present invention can commercially buy, and comprises for example OramixNS10 ex Seppic; Materials such as Plantaren 1200 and Plantaren 2000 ex Henkel.
Can be used for deriving and other next non-ionic surface active agent of the present composition by sugar
Comprise: C
10-C
18N-alkyl (C
1-C
6) polyhydroxy fatty acid amide, for example C
12-C
18N-methyl glucoside amide is described in for example WO 92 06154 and US 5 194 639, and N-alkoxyl polyhydroxy fatty acid amide, for example C
10-C
18N-(3-methoxy-propyl) glucose amide.
The preferred embodiment of cosurfactant is both sexes or zwitterionic surfactant, and its content is 0.5 to about 8%, and preferred 1 to 4% weight is based on total restatement of compositions.
The example of both sexes or zwitterionic surfactant comprises: alkyl amine oxide, alkyl betaine, alkylamide propyl-betaine, alkyl sulfobetaines (sultaine), alkyl glycinate, alkyl carboxyl glycinate, alkyl both sexes acetate, alkyl both sexes propionate, alkyl both sexes glycinate, alkylamide propyl hydroxyl sulfo betaine (alkyl amidopropylhydroxysultaine), acyl taurine salt and acyl glutamate, wherein alkyl and acyl group have 8 to 19 carbon atoms.The typical both sexes and the zwitterionic surfactant that are used for shampoo of the present invention comprise: dodecyl amine oxide, coco dimethyl azochlorosulfonate propyl lycine, empgen BB, cocamido propyl betaine and cocos nucifera oil both sexes sodium acetate.
Particularly preferred both sexes or zwitterionic surfactant are cocamido propyl betaine.
Any mixture of above-mentioned both sexes or zwitterionic surfactant is also applicable.Preferred mixture is the mixture of cocamido propyl betaine and above-mentioned other both sexes or zwitterionic surfactant.Preferred other both sexes or zwitterionic surfactant are cocos nucifera oil both sexes sodium acetates.
The total amount of surfactant in the shampoo compositions of the present invention (comprise all cosurfactants, and/or all emulsifying agents) is generally 1 to 50%, and is preferred 2 to 40%, and more preferably 10 to 25% weight are based on total restatement of compositions.
Cationic polymer
Cationic polymer is a preferred composition in the shampoo compositions of the present invention, is used for improving adjusting function.
Suitable cationic polymer can be a homopolymer, and it is replaced (cationically substituted) by cationic, perhaps can be formed by two or more monomer.Weight average molecular weight (the M of polymer
W) be generally 100 000 to 2 megadaltons.Described polymer has the group of cation nitrogen, for example quaternary ammonium or protonated amino or its mixture.If the molecular weight of polymer is low excessively, then regulating effect is poor.If too high, the problem of high extensional viscosity, the thickness when causing compositions to be toppled over then may appear.
The group of cation nitrogen is present on the part in the whole monomeric units of cationic polymer usually as substituent group.If therefore polymer is not a homopolymer, then it can comprise non-cationic monomeric unit at interval.This polymer is described in CTFA Cosmetic IngredientDirectory (cosmetic composition catalogue), the third edition.Select the ratio of cation and non-cationic monomeric unit, the cationic charge density that makes polymer have required scope it typically is 0.2 to 3.0meq/gm.The cationic charge density of polymer can suitably adopt under the chemical analysis item that is used for nitrogen determination in the American Pharmacopeia described Kjeldahl method to measure.
Suitable cationic polymer comprises: for example, have the vinyl monomer of cationic amine or quaternary ammonium functional group and the copolymer of water solublity spacer monomers (as: (methyl) acrylamide, alkyl and dialkyl group (methyl) acrylamide, (methyl) alkyl acrylate, vinyl caprolactone and ethenyl pyrrolidone).The monomer that alkyl and dialkyl group replace preferably has C
1-C
7Alkyl, more preferably C
1-
3Alkyl.Other proper spacing body comprises: vinyl acetate, vinyl alcohol, maleic anhydride, propylene glycol and ethylene glycol.
Described cationic amine can be primary amine, secondary amine or tertiary amine, depends on the particular category and the pH of compositions.Usually, preferred secondary amine and tertiary amine, special preferred tertiary amine.
Vinyl monomer that amine replaces and amine can amine form carry out polymerization, be converted into ammonium by quaternization then.
Described cationic polymer can comprise by amine-and/or the monomer of quaternary ammonium-substituted and/or compatible spacer monomers derive and the mixture of the monomeric unit that comes.
Suitable cationic polymer comprises, for example:
The polymer of-cation diallyl quaternary ammonium, comprise: for example, the copolymer of dimethyl diallyl ammonium chloride homopolymer and acrylamide and dimethyl diallyl ammonium chloride, (CTFA) is called polyquaternary ammonium salt 6 (Polyquaternium 6) and polyquaternary ammonium salt 7 (Polyquaternium 7) respectively in industry.
-have a mineral acid salt (being described in United States Patent (USP) U.S.Patent 4,009,256) of the aminoalkyl ester of the homopolymer of unsaturated carboxylic acid of 3 to 5 carbon atoms and copolymer;
-PAMC (being described in WO 95/22311).
Other operable cationic polymer comprises the cationic polysaccharide polymer, for example cationic cellulose derivative, cationic starch derivative and cationic guar derivative.
The cationic polysaccharide polymer that is applicable to the present composition comprises the monomer of following formula:
A-O-[R-N
+(R
1)(R
2)(R
3)X
-]，
Wherein: A is the dewatered grape saccharide residue, for example starch or cellulose dewatered grape saccharide residue.R is alkylidene, oxygen base alkylidene, polyoxy alkylidene, or hydroxy alkylidene, or its combination.R
1, R
2And R
3Independently represent alkyl, aryl, alkaryl, aralkyl, alkoxyalkyl, or alkoxy aryl, each group contains up to about 18 carbon atoms.The total number of carbon atoms of each cationic moiety (that is R,
1, R
2And R
3The total number of carbon atoms) preferred about 20 or still less, and X is an anionic counter-ion.
Another kind of cationic cellulose comprises the epoxide reactive polymeric quaternary ammonium salts that hydroxyethyl-cellulose and dodecyl dimethyl ammonium replace, and (CTFA) is called polyquaternary ammonium salt 24 (Polyquaternium 24) in industry.These materials can be available from Amerchol company (for example trade name Polymer LM-200).
Other suitable cationic polysaccharide polymer comprises the cellulose ether (for example being described in United States Patent (USP) U.S.Patent 3,962,418) that contains quaternary nitrogen, and the copolymer of etherified cellulose and starch (for example being described in United States Patent (USP) U.S.Patent 3,958,581).
The cationic polysaccharide polymer type of operable particularly suitable is a cationic guar derivative, for example guar gum hydroxypropyl-trimethyl ammonium chloride (can available from the JAGUAR trade mark series of Rhodia).This examples of substances is JAGUAR C13S, JAGUAR C14, JAGUAR C15 and JAGUAR C17.
Also can use the mixture of above-mentioned cationic polymer.
The amount of cationic polymer is generally 0.01 to 5% of compositions gross weight with the total restatement of cationic polymer in the shampoo compositions of the present invention, and is preferred 0.05 to 1%, more preferably 0.08 to 0.5% weight.
Suspending agent
Preferably, aqueous shampoo compositions of the present invention also comprises suspending agent.Suitable suspending agent can be selected from: the cross-linked copolymer of the copolymer of polyacrylic acid, acrylic acid cross linked polymer, acrylic acid and hydrophobic monomer, the copolymer that contains carboxylic acid monomer and acrylate, acrylic acid and acrylate, heteropolysaccharide glue and crystalline long acyl derivant.Described long acyl derivant be selected from ideally ethylene glycol stearate, have an alkanolamide and composition thereof of the fatty acid of 16 to 22 carbon atoms.Glycol distearate and Polyethylene Glycol 3 distearates are preferred long acyl derivants, because they can make compositions have pearly-lustre (pearlescence).Polyacrylic acid can be purchased and be Carbopol 420, Carbopol 488 or Carbopol 493.Can also use the cross linked polymer of acrylic acid and multiple functional radical reagent; They can be purchased and be Carbopol 910, Carbopol 934, Carbopol 941 and Carbopol 980.The example that contains the suitable copolymer of carboxylic acid monomer and acrylate is Carbopol 1342.All Carbopol (trade mark) material can be available from Goodrich.
The suitable cross linked polymer of acrylic acid and acrylate is Pemulen TR1 or PemulenTR2.Suitable heteropolysaccharide glue is xanthan gum, and for example it can purchase the mu into Kelzan.
Can use any mixture of above-mentioned suspending agent.The mixture of acrylic crosslinking polymer and crystalline long acyl derivant preferably.
The amount of suspending agent is generally 0.1 to 10% of compositions gross weight with the total restatement of suspending agent in the shampoo compositions of the present invention, and is preferred 0.5 to 6%, and more preferably 0.9 to 4%.
Regulating composition
Regulating composition comprises one or more cation reconciliation statement surface-active agents usually, and it is acceptable and be applicable to the hair topical application on the cosmetics.
Preferably, described cation reconciliation statement surface-active agent has formula N
+(R
1) (R
2) (R
3) (R
4), R wherein
1, R
2, R
3And R
4Independent is (C
1To C
30) alkyl or benzyl.
Preferably, R
1, R
2, R
3And R
4In one, two or three independently are (C
4To C
30) alkyl, and R
1, R
2, R
3And R
4Other group in the group is (C
1To C
6) alkyl or benzyl.
More preferably, R
1, R
2, R
3And R
4In one or two independently is (C
6To C
30) alkyl, and R
1, R
2, R
3And R
4Other group in the group is (C
1To C
6) alkyl or benzyl.Randomly, can comprise in the alkyl chain of described alkyl one or more ester bonds (OCO-or-COO-) and/or ehter bond (O-).Alkyl can be chosen wantonly by one or more hydroxyls and replace.Alkyl can be a straight or branched, and for the alkyl that contains 3 or more carbon atoms, can be cyclic.Described alkyl can be saturated or can comprise one or more carbon-carbon double bonds (for example oleyl).Alkyl can be chosen wantonly and the ethoxylation on alkyl chain of one or more ethyleneoxies.
The suitable cation reconciliation statement surface-active agent that is used for regulating composition of the present invention comprises: hexadecyltrimethylammonium chloride, INCROQUAT TMC-80 ECONOL TM22, hexadecylpyridinium chloride, tetramethyl ammonium chloride, tetraethylammonium chloride, the octyl group trimethyl ammonium chloride, Dodecyl trimethyl ammonium chloride, hexadecyltrimethylammonium chloride, octyldimethyl benzyl ammonium chloride, decyl dimethyl benzene ammonio methacrylate, octadecyl dimethyl benzene ammonio methacrylate, two dodecyl dimethyl ammonium chloride, dioctadecyl dimethyl ammonium chloride, the Adeps Bovis seu Bubali trimethyl ammonium chloride, two hydrogenated tallow alkyl dimethyl ammonium chlorides (for example, from Akzo Nobel Arquad 2HT/75), the cocos nucifera oil trimethyl ammonium chloride, PEG-2 oil base ammonio methacrylate (PEG-2-oleammoniumchloride) and corresponding hydroxide thereof.Other cationic surfactant that is suitable for comprises that those CTFA are called the material of quaternary ammonium salt-5 (Quaternium-5), quaternary ammonium salt-31 (Quaternium-31) and quaternary ammonium salt-18 (Quaternium-18).Any mixture of above-mentioned substance is also applicable.The useful especially cationic surfactant that is used for regulator of the present invention is a hexadecyltrimethylammonium chloride, and the commercially available prod has, GENAMIN CTAC for example, ex Hoechst Celanese.Other the useful especially cationic surfactant that is used for regulator of the present invention is an INCROQUAT TMC-80 ECONOL TM22, and the commercially available prod has, GENAMIN KDMP for example, ex Clariant.
Other type example that is used for suitable cation reconciliation statement surface-active agent of the present invention uses separately or mixes use with one or more other cation reconciliation statement surface-active agents, is following (i) and combination (ii):
(i) corresponding to the amidoamines of general formula (I)
R wherein
1For having the hydrocarbyl chain of 10 or more carbon atoms,
R
2And R
3Independently be selected from hydrocarbyl chain with 1 to 10 carbon atom, and
M is 1 to about 10 integer; With
(ii) a kind of acid.
As used herein, term " hydrocarbyl chain " is meant the alkyl or alkenyl chain.
Preferred amidoamines chemical compound is those materials corresponding to formula (I), wherein
R
1For having about 11 hydrocarbyl residue to about 24 carbon atoms,
R
2And R
3Independent separately is hydrocarbyl residue, preferably has 1 alkyl to about 4 carbon atoms, and
M is 1 to about 4 integer.
Preferably, R
2And R
3Be methyl or ethyl.
Preferably, m is 2 or 3, that is, and and ethylidene or propylidene.
Preferred amidoamines used herein comprises the stearamide propyl dimethyl amine, the stearamide propyl diethylamide, stearmide ethyl diethylamide, stearmide ethyl dimethyl amine, the palmitamide propyl-dimethyl amine, palmitamide propyl group diethylamide, palmitamide ethyl diethylamide, palmitamide ethyl dimethyl amine Shan Yu amido propyl dimethyl amine Shan Yu amido propyl diethylamide Shan Yu amide ethyl diethylamide Shan Yu amide ethyl dimethyl amine, arachidonic amido propyl dimethyl amine, arachidonic amido propyl diethylamide, arachidonic amide ethyl diethylamide, arachidonic amide ethyl dimethyl amine, and composition thereof.
Particularly preferred amidoamines used herein is stearamide propyl dimethyl amine, stearmide ethyl diethylamide, and composition thereof.
Can the commercial amidoamines of buying used herein comprise: can be available from Inolex (Philadelphia, Pennsylvania, the U.S.) the stearamide propyl dimethyl amine of commodity LEXAMINE S-13 by name, and can be available from Nikko (Tokyo, Japan) AMIDOAMINE MSP, can be called the stearmide ethyl diethylamide of AMIDOAMINE S available from the commodity of Nikko, can be available from Croda (North Humberside, Britain) the mountain Yu amido propyl dimethyl amine of commodity INCROMINE BB by name, and can be available from Scher (Clifton, the various amidoamines of the SCHERCODINE series by name of commodity New Jersey, U.S.).
Acid (ii) can be any protonated organic acid or mineral acid of amidoamines that can make in the hair-treatment composition.Suitable acid used herein comprises: hydrochloric acid, acetic acid, tartaric acid, fumaric acid, lactic acid, malic acid, succinic acid, and composition thereof.Preferably, described acid is selected from: acetic acid, tartaric acid, hydrochloric acid, fumaric acid, and composition thereof.
The main effect of described acid is to make the amidoamines in the hair-treatment composition protonated, thereby the original place forms tertiary ammonium salt (TAS) in hair-treatment composition.TAS is actually impermanency quaternary ammonium or false quaternary ammonium cation surfactant.
Suitably, the amount of described acid should be enough to make all amidoamines of existence protonated, that is, its consumption at least with compositions in the mole such as amount of existing amidoamines.
In regulator of the present invention, the amount of cation reconciliation statement surface-active agent is generally 0.01 to 10% of compositions gross weight with the total restatement of cation reconciliation statement surface-active agent, and more preferably 0.05 to 7.5%, most preferably 0.1 to 5%.
Regulator of the present invention also comprises aliphatic alcohol usually.Be used in combination aliphatic alcohol and cationic surfactant is considered to advantageous particularly in treatment compositions, because this causes the formation of lamellar phase, and cationic surfactant is scattered in wherein.
Representative fatty alcohols comprises 8 to 22 carbon atoms, more preferably 16 to 22.Aliphatic alcohol normally contains the chemical compound of straight chained alkyl.Suitably the example of aliphatic alcohol comprises: cetyl alcohol, stearyl alcohol and composition thereof.Use the benefit of these materials to be that also they help the overall adjustment characteristic of the present composition.
The amount of aliphatic alcohol is generally 0.01 to 10% in the regulator of the present invention, and is preferred 0.1 to 8%, and more preferably 0.2 to 7%, most preferably 0.3 to 6%, based on the weight meter of compositions.The weight ratio of cationic surfactant and aliphatic alcohol is 1:1 to 1:10 suitably, is preferably 1:1.5 to 1:8, and the best is 1:2 to 1:5.If the weight ratio of cationic surfactant and aliphatic alcohol is too high, this can cause the stimulation of compositions to eyes.If weight ratio is low excessively, this can make some consumer's sensation hair crude (squeaky).
Hair oil and shampoo
The present composition can suitably adopt the form of hair oil, for washing preceding or washing the back and use.Usually, hair oil mainly comprises water-insoluble oily adjusting material, for example triglyceride, mineral oil and composition thereof.
The present composition can also adopt the form of shampoo, uses between twice hair washing usually.Washing liquid is the water-based emulsion that comprises water-insoluble oily instrumentality matter.Shampoo also can comprise suitable surfactant, to improve the stability to being separated.
The silicone regulator
Hair-treatment composition of the present invention particularly based on the shampoo and the hair conditioner of water, also preferably comprises one or more silicone regulators.
Particularly preferred silicone regulator is a silicone emulsion, those emulsions that form by following silicone for example, polydiorganosiloxanepolyurea for example, particularly CTFA is called the polydimethylsiloxane of simethicone (dimethicone), polydimethylsiloxane with CTFA diformazan silica alkanol (dimethiconol) by name of C-terminal, and the amino-functional polydimethylsiloxane of CTFA ammonia end polydimethylsiloxane (amodimethicone) by name.
Sauter average droplet size (the D of emulsion droplets described in the present composition
3,2) be generally 0.01 to 20 micron, more preferably 0.2 to 10 micron.
Measure Sauter average droplet size (D
3,2) proper method, be by laser light scattering, use instrument as Malvern Matersizer.
The suitable silicone emulsion that is used for the present composition can obtain from silicone supplier (for example DowCorning and GE Silicones).Owing to easily process and control silicone particle diameter, so preferably use prefabricated silicone emulsion.This prefabricated silicone emulsion also comprises suitable emulsifying agent usually; for example anion or nonionic emulsifier; or its mixture, and can prepare by chemical emulsification technology (as the emulsion polymerisation effect), perhaps use high-shear mixer to prepare by machinery emulsification.Sauter average droplet size (D
3,2) be commonly called microemulsion less than 0.15 micron prefabricated silicone emulsion.
The example of suitable prefabricated silicone emulsion comprises emulsion DC2-1766, DC2-1784, DC-1785, DC-1786, DC-1788 and microemulsion DC2-1865 and DC2-1870, all can be available from Dow Corning.These all are the emulsion/microemulsion of diformazan silica alkanol.Ammonia end polydimethylsiloxane (amodimethicone) emulsion is also applicable, for example DC2-8177 and DC939 (from Dow Corning) and SME253 (from GE Silicones).
It is also applicable that wherein the high molecular weight surface reactive block copolymers of some type and silicone emulsion drip blended silicone emulsion, is described in for example WO 03/094874.In these materials, silicone emulsion drips preferably and is formed by those for example above-mentioned polydiorganosiloxanepolyureas.A kind of surface activity block copolymer of preferred form is according to following formula:
HO(CH
2CH
2O)
x(CH(CH
3)CH
2O)
y(CH
2CH
2O)
xH
Wherein the meansigma methods of x is 4 or bigger, and the meansigma methods of y is 25 or bigger.
The surface activity block copolymer of another kind of preferred form is according to following formula:
(HO(CH
2CH
2O)
a(CH(CH
3)CH
2O)
b)
2-N-CH
2-CH
2-N((OCH
2CH(CH
3))
b(OCH
2CH
2)
aOH)
2
Wherein the meansigma methods of a is 2 or bigger, and the meansigma methods of b is 6 or bigger.
Also can use any mixture of above-mentioned silicone emulsion.
The amount of above-mentioned silicone emulsion in the present composition is generally 0.05 to 10% of compositions gross weight with the total restatement of silicone, and be preferred 0.05 to 5%, and more preferably 0.5 to 2%.
Other optional ingredients
The present composition can comprise other composition, to improve performance and/or consumer's acceptability.These compositions comprise: aromatic, dyestuff and pigment, pH regulator agent, pearling agent (pearlescers) or opacifier, viscosity modifier, and antiseptic or antimicrobial.The amount of every kind of these compositions can effectively be realized its purpose.Usually each plant demand of these optional members can reach 5% of compositions gross weight.
Occupation mode
Hair-treatment composition of the present invention mainly supplies the topical application of human hair and/or scalp, can be the compositions of wash type or conservative, can be used for drying, the impaired and/or difficult processing of arranging (unmanageable) hair.
Will the invention will be further described by following unrestricted embodiment, except as otherwise noted, wherein all percents of Ti Chuing all are based on the percetage by weight of total restatement.
Embodiment
Preparation has the prescription of composition shown in the following table 1.
Table 1
Use grading system sense organ methodology (rank sensory methodology), the multinomial performance feature of embodiment 1 prescription and control formula is compared.
Use embodiment 1 prescription and control formula respectively, to handling through bleaching and painted Chinese wig (Chinese hair switches).
By 12 group members the wig after handling is assessed.The group member is at following four organoleptic attributes: termination neat (tip alignment), slickness, easy cardability and dry terminal, mark to the wig after handling with embodiment 1 prescription with the wig after the control formula processing.
With Friedman two factor variance analyses (Friedman ' s two-way ANOVA) to the sensorial data analysis of marking.
Result's (average score of every kind of test formulations) is as shown in table 2 below:
Table 2
| Organoleptic attribute | The average score of contrast | The average score of embodiment 1 |
| The termination neat | 2.75 | 2.75 |
| Slickness | 1.96 | 2.67 |
| Easy cardability | 1.79 | 2.92 |
| Dry terminal | 3.21 | 1.96 |
Organoleptic attribute scoring direction is as follows:
The termination neat: it is high more good more to mark
Slickness: it is high more good more to mark
Easy cardability: it is high more good more to mark
Dry terminal: it is low more good more to mark
The result shows that compared with the control, embodiment 1 prescription has suitable termination neat, preferably slickness, significantly (〉 95%) easy cardability preferably, and remarkable (〉 95%) reduced dry end.
Claims (8)
1. hair-treatment composition, it comprises sugar, amine oxide and amino acid whose combination.
2. the hair-treatment composition of claim 1, wherein said sugar is aldohexose.
3. the hair-treatment composition of claim 2, wherein said aldohexose is a galactose.
4. each hair-treatment composition in the aforementioned claim, wherein said amine oxide are alkyl two-(low alkyl group) amine oxides.
5. the hair-treatment composition of claim 4, wherein said amine oxide is a decyl dimethyl oxidation amine.
6. each hair-treatment composition in the aforementioned claim, wherein said aminoacid is basic amino acid.
7. the hair-treatment composition of claim 6, wherein said aminoacid is arginine.
8. each hair-treatment composition in the aforementioned claim, its form be shampoo, wash back regulator (conservative or wash type), hair oil or shampoo.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05257773 | 2005-12-16 | ||
| EP05257773.1 | 2005-12-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101370469A true CN101370469A (en) | 2009-02-18 |
Family
ID=36337431
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2006800527032A Pending CN101370469A (en) | 2005-12-16 | 2006-12-07 | Hair treatment compositions |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20090232759A1 (en) |
| EP (1) | EP1959916A1 (en) |
| JP (1) | JP2009519270A (en) |
| CN (1) | CN101370469A (en) |
| BR (1) | BRPI0620703A2 (en) |
| CA (1) | CA2633816A1 (en) |
| RU (1) | RU2008129097A (en) |
| WO (1) | WO2007068398A1 (en) |
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|---|---|---|---|---|
| EP3154506A1 (en) | 2014-06-16 | 2017-04-19 | The Procter & Gamble Company | Method of treating hair with a concentrated conditioner |
| JP6633004B2 (en) | 2014-06-16 | 2020-01-22 | ザ プロクター アンド ギャンブル カンパニーＴｈｅ Ｐｒｏｃｔｅｒ ＆ Ｇａｍｂｌｅ Ｃｏｍｐａｎｙ | Method for treating hair using a thickening conditioner |
| BR112016029264A2 (en) | 2014-06-16 | 2017-08-22 | Procter & Gamble | Method for treating hair with a concentrated conditioner |
| CN107847767A (en) * | 2015-04-23 | 2018-03-27 | 宝洁公司 | Hair-care care composition |
| KR101799368B1 (en) * | 2015-07-17 | 2017-11-20 | 주식회사 토리파인스 | Detergent composition having a treatment function |
| CN108367168A (en) | 2015-12-15 | 2018-08-03 | 宝洁公司 | The method for handling hair |
| US10322072B2 (en) | 2015-12-15 | 2019-06-18 | The Procter And Gamble Company | Method of treating hair |
| US10124951B2 (en) | 2015-12-15 | 2018-11-13 | The Procter And Gamble Company | Method of treating hair |
| MX371218B (en) | 2015-12-15 | 2020-01-08 | Procter & Gamble | Method of treating hair. |
| US10265251B2 (en) | 2015-12-15 | 2019-04-23 | The Procter And Gamble Company | Method of treating hair |
| WO2017106404A1 (en) | 2015-12-15 | 2017-06-22 | The Procter & Gamble Company | Method of treating hair |
| US10835480B2 (en) | 2016-04-22 | 2020-11-17 | The Procter And Gamble Company | Method of forming a silicone layer |
| WO2017184794A1 (en) | 2016-04-22 | 2017-10-26 | The Procter & Gamble Company | Method of forming a silicone layer |
| US11464724B2 (en) | 2018-11-08 | 2022-10-11 | The Procter & Gamble Company | Low shear stress conditioner composition with spherical gel network vesicles |
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- 2006-12-07 US US12/086,450 patent/US20090232759A1/en not_active Abandoned
- 2006-12-07 EP EP06840961A patent/EP1959916A1/en not_active Withdrawn
- 2006-12-07 CN CNA2006800527032A patent/CN101370469A/en active Pending
- 2006-12-07 RU RU2008129097/15A patent/RU2008129097A/en not_active Application Discontinuation
- 2006-12-07 WO PCT/EP2006/011811 patent/WO2007068398A1/en active Application Filing
- 2006-12-07 BR BRPI0620703-0A patent/BRPI0620703A2/en not_active IP Right Cessation
- 2006-12-07 CA CA002633816A patent/CA2633816A1/en not_active Abandoned
- 2006-12-07 JP JP2008544828A patent/JP2009519270A/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US20090232759A1 (en) | 2009-09-17 |
| WO2007068398A1 (en) | 2007-06-21 |
| CA2633816A1 (en) | 2007-06-21 |
| JP2009519270A (en) | 2009-05-14 |
| RU2008129097A (en) | 2010-01-27 |
| EP1959916A1 (en) | 2008-08-27 |
| BRPI0620703A2 (en) | 2011-11-22 |
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